Curing agents for epoxy resins



United States Patent 3,408,215 Patented Oct. 29, 1968 3,408,215, CURING AGENTS FOR EPOXY RESINS Marco Wismer, Gibsonia, and John R. Peifer, Verona, Pa., assignors to Pittsburgh Plate Glass Company, Pittsburgh, Pa., a corporation of Pennsylvania No Drawing. Filed June 26, 1964, Ser. No. 378,414 16 Claims. (Cl. 106-252) ABSTRACT OF THE DISCLOSURE Novel storage-stable curing agents for epoxide resins are obtained by esterifying an admixture of polyol, nonhalogenated polycarboxylic acid, and halogenated polycarboxylic acid in the presence of an aliphatic diol having 2 to' IOcarbon'atoms and solubilizing the ester in a solvent. These curing agents give improved flexibility and harder cures to the epoxide resin coating systems.

closed in US. Patent 3,050,480 utilizes epoxidized drying oils derived from vegetable, animal, and marine sources which have been epoxidized with peracetic acid or other means. This type of epoxy resin coating system can be applied in thin films to form hard, mar-resistant, cor-' rosion-resistant coatings.

One type of epoxy resin system utilized comprises an epoxidized long chain fatty acid or ester thereof having an iodine value of at least 90 before epoxidation and after epoxidation containing not less than 4 percentoxirane groups located within the molecules of said fatty acid chain material.

Curing of these epoxidized oils has been accomplished by using polycarboxylic acids of various types,- such as monochlorophthalic acid, tetrachlorophthalic acid, and hexachloroendomethylenetetrahydrophthalic acid (chlorendic acid). A

While the coating systemsdisclosed in US. Patent 3,050,480 are useful, a further modification has been introduced wherein esters of polycarboxylic acids and polyols, said esters having a minimum of two free carboxyl groups per molecule, have been substituted for the acid curing agents of the above patent. The carboxyl terminated esters, when used as curing agents for epoxidized vegetable oils, give improved flexibility and harder cures to the coating systems.

These carboxyl terminated esters are generally nonpolymeric in nature, i.e., each of the OH groups of a polyol is reacted with a carboxyl group of a polycarboxylic acid, the other carboxyl groups of that acid molecule remaining unreacted. The structural representation of these carboxyl terminated esters is as follows:

wherein R is an organic group containing only carbon, hydrogen, nitrogen, and oxygen, preferably an open chained organic group having 2 to carbon atoms, such as an alkyl group of 2 to 15 carbon atoms, alkoxyalkyl groups having 4 to 15 carbon atoms, and the like, repre senting the backbone of a polyol, A is an organic hydrocarbon group, preferably a mono-nuclear cyclic group having 6 cyclic carbon atoms, and x is a whole number from 2 to 6 although preferably from 2 to 4, which represeats the number of carboxyl groups per ester as well as the hydroxyl functionality of the polyol.

A further advantage of the carboxyl terminated esters resides in the fact that acids such as phthalic, isophthalic, terephthalic, and the like can be utilized in preparing these esters although such acids are not suitable when utilized as the sole curing agent for epoxidized vegetable oils. Phthalic, terephthalic, and isophthalic acids are not strong enough per se to promote rapid cure of epoxidized vegetable oils; therefore, in the carboxyl terminated esters described above, it is preferred to utilize a chlorinated acid as a portion of the polycarboxylic acid reactant.

Although the carboxyl terminated esters are advantageously utilized as curing agents for epoxidized oils, such esters are frequently unstable during storage. Esters prepared from a polyol and a mixture of non-halogenated polycarboxylic acids and halogenated polycarboxylic acids, such as mixtures of phthalic acid and hexachloroendomethylenetetrahydrophthalic acid, frequently form precipitates form precipitates after standing in solution for a period of days. This precipitate is undesirable in a curing agent solution.

It has now been discovered that a storage stable solution comprising a carboxyl terminated ester prepared i from a polyol, a nonhalogenated polycarboxylic acid containing 2 to about 12 carbon atoms, preferably a mononuclear cyclic polycarboxylic acid having 6 cyclic carbon atoms, and a halogenated polycarboxylic acid containing about 3 to about 12 carbon atoms, preferably a cyclic polycarboxylic acid having at least 6 cyclic carbon atoms,

said nonhalogenated polycarboxylic acid being present in a ratio of moles of acid to equivalents of polyol of about 0.05:1 to about 0.75:1, said halogenated polycarboxylic acid being present in such quantity as to have a ratio of total moles of acid to equivalents of polyol of about 0.6:1 to about 1.2:1, wherein any non-halogenated polycarboxylic acid which is initially unreacted with the polyol or later becomes displaced from said polyol, is at least partly esterified with an aliphatic diol having 2 to 10 carbon atoms.

The carboxyl terminated ester always contains at least 0.05 :1 moles of halogenated polycarboxylic acid to equivalents of polyol, and at the lower levels of total acid to polyol, for example, 0.621, the halogenated polycarboxylic acid is present at about 0.3:1 moles of halogenated polycarboxylic acid to equivalents of polyol. The amount of halogenated acid required is inversely proportional to the total quantity of acid present per equivalent of polyol. Of course, higher levels of halogenated polycarboxylic acid may be utilized at the higher ratios of total acid to priate solvent such as those hereinafter disclosed, is storage stable, i.e., does not form an undesirable precipitate and has improved pot life when admixed with an epoxidized oil to form a coating composition without adversely affecting the curing time of films prepared therefrom.

A novel method for preparing the storage stable solution of the carboxyl terminated ester described above involves the following steps:

(1) heating an admixture of a polyol, preferably one having a functionality greater than two, a nonhalogenated 'polycarboxylic acid having 2 to 12 carbon atoms, and a halogenated polycarboxylic acid having 3 to 12 carbon atoms to a temperature of about C. to about 250 C., preferably about C to about 200 C., to effect esterification, said non-halogenated polycarboxylic acid prefabout 180 C., preferably at about 150 C.-to about 165 C., while adding about 1.0 percent by weight to about 8.0 percent by weightvof a diol based upon the weight of ester present. The-resulting admixture can be cooled and dissolved in an appropriate solvent such as a mixture-of higher boiling aliphatic hydrocarbons and the monomethyl ether of ethylene glycol acetate.

The above technique, substantially a fusion process, is preferably practiced by admixing the nonhalogenated polycarboxylic acid and the polyol initially and heating to a teinperatureof about 100 C. to about 250 C. prior to the addition of the halogen containing polycarboxylic acid;

As-mentioned' above, the ester is preferably prepared by having the'halogenated polycarboxylic acid present as about 20 mole percent to about 90 mole percent of the total acid present.

The process may also be carried out in a manner similar to that outlined above, but in the presence of a suitable solvent. Suitable solvents include:

toluene petroleum naphtha higher boiling aromatic solvents, i.e., those boiling above about 130 C., e.g., xylene higher boiling aliphatic solvents, i.e., those boiling above about 130 C.

and the like 4 While it is preferred to add the diol at the conclusion of the esterification reaction, the novel process can also.

be practiced by adding the diol during or before the initial esterification step. This procedure has the advantage of eliminating the separate. step described hereinabove for diol addition. The carboxyl terminated esters prepared by this alternate method are comparable to those prepared by the method described hereinabove.

, The carboxyl terminated ester is dissolved in a suitable solvent for use as a curing-agent for epoxidized drying oils. Such solvents include:

toluene n higher boiling aromatic solvents, i.e., those boiling above about 130 C. such as xylene, naphthalene, and the like,

ketones such as methyl ethyl ketone, methyl isobutyl ke-i tone, and the like, esters such as butyl acetate, amyl acetate, octyl acetate,

and the like, ethers such as ethylene glycol monobutyl ether, ethylene glycol monobutyl ether acetate, ethylene glycol monoethyl ether acetate, ethylene glycol monomethyl ether acetate,

and the like. Polycarboxylic acids useful in the instant invention preferably contain 2 to 12 carbon atoms and include:

dichloromaleic acid "monochlorophthalic acid v those having a. so lubil ity,of.less than 2.0,grarr'is per-. 100

grams-of ethyl ether. Ofitheabove nonhalogenated polycarboxylic acids, phthalivacidand: its'anh'ydride are generally preferred for utilizationjn these esters. It is significant that the precipitation problem is most acute with phthalic acid and its" anhydrid;'t'herefore, "the novel techniques of this invention have their greatest applicability, to carboxyl terminated esters containing phthalic acid.

When tetr'ahydrophthalic areusedfas 'the'nonhalogenated acids in the preparation of the'ca'rboxyl terminated esters ofthis invention, no precipitation from solution occurs; however, the treatment with diols improves thetpot-lifeof epoxidized 'oil'resins which have been catalyzed with carboxyl terminated esters of such acids.

1 I The polyols which are utilized as the backbone of the carboxyl terminated esters of this inventioncontain from about 2 to about 6 hydroxyl groups. Such polyols include ethylene glycol propylene glycol diethylene glycol dipropylene glycol trimethylolproprane trim'ethylolethane pentaerythritol dipentaerythritoli tripentaerythritol glycerol 1,2,6-hexanetriol i I ,1

butylene glycol triethylene glycol neopentyl-glycol' mannitol sorbitol diethanolamine' triethanolamine triisopropylamine w N,N,N'N'-tetrakis(hydroxypropyl)ethylenediamine" andthelike. V, i" I j f Aliphatic polyols having a hydroxyl funct'ion al ityofv greater than 2 and from 3 to about 15 carbon'a'toms are preferred for the purposes of this invention. I c

f The diols used to stabilize the carboxyl termi ated esters include aliphatic diols of Z'to lOcarborr atoms such as; L

" ethylene glycol neopentyl glycol.

propylene glycol neopentyl glycol 1,3 propanediol; 1,4 butane diol diethylene glycol dipropylene glycol and the "like. The preferred di'ols are ethylene glycol e type described In Clllil'lgfiPOXidiZt-id drying'oils of epoxide resin such as: bis(4-glycidoxyphenyl)-2,2-propane bis(4-glycidoxyphenyl)-1,l-ethane hereinabove, it is'preferred to include a' conventional bis(4-glyci doxyphenyl)-2,2-butane.

v l-chloro-2,3-epoxy propane bis(3,4-epoxy-6-methylcyclohexylmethyl) adipate limonene dioxide and the like.

The following preparation illustrates the conventional method of preparing a carboxyl terminated ester which is suitable for curing epoxidized oils of the type mentioned hereinabove.

PREPARATION A.An ester curing agent was prepared from the following ingredients:

Phthalic anhydride 133 grams (0.9 mole). Pentaerythritol 68 grams (0.5 mole). Hexachloroendomethyle n e t e t r ahydrophthalic acid (chlorendic acid) 389 grams (1.0 mole). Solvent 1 50 milliliters.

1 Solvent is Solvesso 100, an aromatic hydrocarbon mixture having a boiling point range of 150 C. to 170 C.

Phthalic anhydride, pentaerythritol, and Solvesso 100 were admixed in a reaction vessel equipped with a stir-. rer, reflux condenser, temperature measuring device, inert gas sparge tube, and moisture trap. These ingredients were heated to about 150 C. At this temperature about one-third of the chlorendic acid was added. The heating and stirring was continued for about 10 additional minutes before an additional one-third of the chlorendic acid was added. The mixture was then heated for approxiproximately minutes more before the final addition of chlorendic acid was made.

The mixture was heated further to a temperature of about 175 C. This temperature was maintained until all the water of reaction had been collected in the moisture trap. The temperature was then lowered to about 160 C. at which temperature about 104 milliliters of the mono ethyl ether of ethylene glycol acetate and 330 milliliters of Solvesso'100 were added.

The product had a final acid value of about 109, a color (Gardner) of 4, a viscosity (Gardner-Holdt) of U to V, a solids content of 60.7 percent, and a free anhydride content of 3.96 percent.

After standing for 1 week, the solution was cloudy;

After about 10 days the solution was very cloudy, in;

dicating precipitation.

The following examples illustrate in detail the'novel features of this invention. The examples are not intended to limit the invention, however, for there are, of course, numerous possible variations and modifications.

EXAMPLE I A stable ester curing agent was prepared from the following ingredients:

Phthalic anhydride 133 grams (0.9 mole). Pentaerythritol 68 grams (0.5 mole). Hexachloroendomethyle n e t e tr ahydrophthalic acid (chlorendic acid) 389 grams (1.0 mole). Solvent 1 milliliters.

1 Solvent is Solvesso 100. an aromatic hydrocarbon mixture having a boiling point range of 150 C. to 170 C.

The phthalic anhydride, pentaerythritol, and solvent were admixed in a reaction vessel equipped similarly to that used in Preparation A. The admixture was heated to about 150 C. at which temperature about one-third of the chlorendic acid was added. The chlorendic acid was added incrementally over a period at about 20 minutes while maintaining the temperature at about 150 C. to about 160C. The temperature of the mixture was thenrais'ed to about 175 C., the water of esterification being collected. When all the water of esterification had been removed, the mixture was allowed to cool. At about a temperature of 160 C., about 23 grams of ethylene glycol were added. The temperature was maintained at about 160 C. for about one-half hour. The reaction mixture was then thinned in a solvent mixture of 104 6. milliliters of the monoethyl ether of ethylene glycol acetate and 330 milliliters of Solvesso 100.

The final product had an acid value of 94.2 without water, an acid value of 97.8 with Water, a color of 2 (Gardner), a viscosity of V to W (Gardner-Holdt), a solids content of 60.8 percent, and a phthalic anhydride content of 0.95 percent as calculated from the difference in acid values determined with and without added water. This mixture was stable upon storage. No precipitate was evident after one months storage of several samples in a cold room, a hot room, and at room temperature.

EXAMPLE II A stable ester curing agent was prepared using trimethylolpropane to stabilize the ester:

Grams Phthalic anhydride 665 Pentaerythritol 340 Chlorendic acid 1945 The phthalic anhydride, pentaerythritol, and about onethird of the chlorendic acid were admixed in a reaction 160 C. at which temperature about 80 grams of trimethylolpropane were added. The temperature was maintained at about 160 C. for about 3 0 minutes before about 1020 milliliters of Solvesso 100 and 780 milliliters of the monoethyl ether of ethylene glycol acetate were added.

After filtering the reaction product, it had an acid value of 110, solids content of 67.5, viscosity of Y to z (Gardner-Holdt), and a color about 4+ (Gardner).

After storage of several samples for 20 days in a cold room, hot room, and at room temperature, no precipitate was observed in any of the samples.

EXAMPLE HI A stable ester curing agent was prepared using neo-' pentyl glycol as a stabilizing ingredient.

Phthalic anhydride 133 grams (0.9 mole).

Pentaerythritol 68 grams (0.5 mole). Chlorendic acid 389 grams 1.0 mole). Solvent 1 50 milliliters.

ture having a boiling point range of C. to C.

The pht halic anhydride, pentaerythritol, and solvent were charged to a reaction vessel equipped similarly to that utilized in Preparation A. The admixture was heated to a temperature of about 170 C. at which temperature about one-third of the chlorendic acid was added. The chlorendic acid was added incrementally over a period of about 20 minutes while the temperature was maintained at about C. The reaction mixture continued to be heated until all the water of reaction was removed. The reaction mixture was cooled to a temperature of about 140 C. at which temperature about 25 grams of neopentyl glycol were added. The temperature was maintained at about 150 C. for about one-half hour.

At a temperature of about 140 C., an admixture of monoethyl ether of ethylene glycol acetate (104 milliliters) and Solvesso 100 (300 milliliters) was added.

After filtering, the reaction product had an acid value of 97.2, a viscosity of X to Y (Gardner-Holdt), a color of 3 (Gardner), and solids content of 62.6 percent.

EXAMPLE IV To determine the effect upon pot-life of a catalyzed, epoxidized oil, the following tests were performed:

Several samples of an epoxidized oil resin containing 4.5 parts by weight of an epoxidized soya oil having an to equivalents of poly-o1 of about 0.05:1 to about 0.75 :1, oxirane oxygen content of 5.8 percent (ep oxide equivasaid halogenated polycarboxylic acid being present in such lent weight of 276) and 0.5 part ,byweight of EP.201 quantity as to have a ratio of total moles of'acid to (3,4 epoxy 6 methylcyclohexylmethyl -3,4 epoxyequivalents of polyol of about 0.6:1-to' about 1.2:1, 6 methylcyclohexane carboxylate) dissolve-d in a mixture wherein any nonhalogenated polycarboxylic acid 'unreof 5.0 parts by weight of Solvesso 100 (aromatic hydroacted with said polyol is at least partly esterified with an carbon mixture having a boiling point range of 150 C. aliphatic diol having 2 to carbon atoms, and '(2) a' to 170 C.) and .1.7 parts by weight of the monoethyl solvent for said ester. ether of ethylene glycolacetate, werecatalyzed with vari- I 2. A curing agent solution for epoxide; resins com-. ous catalysts (carboxyl terminated esters). 1 1O prising (1) an. ester prepared from an-aliphatic polyol having. a hydroxyl functionality from about-2 to about e g 6 and containing 3 to about carbon atoms,.a nonsample Curing Agent achieva Geltime chlorinated mononuclear cyclic polycarboxylic acid'havtrack-free -l ing .6 cyclic carbonatoms and a chlorinated cyclic polycondition hours (hm) 15 carboxylic acid having at least 6 cyclic carbon atoms, A. 8.3 parts 'by weight 5.0 'parts by 1.75 94 v, p g R W- 3 and b present wg ght r 5011,15) r a ca boxyl a ra 10 0 mo es.o acid to equivalents-to p0 yol of about .g e gfi g g gg lg .zggg zgg 0.05 :1 to about 0.75 :1, said chlonnated polycarboxylic i i iii l l fi t g g g g, peg; h acid being present in such quantity as to have a ratio ae o, eray rop caci r and solubilized in a mixture otsol- 1 g g moles to eqinvialents o POIYOYI 'z I, x g er r a gfig m Bmpmmn i51 torabou td 1.2.1, wh(ere1n k any rdioncililorlmated polycar oxy 1c aci unreacte wit sai po yo is at' east B 8.3 arts by we1ght'5.0 arts by 1.5 192 I wigltdof p fi pf 5 ggxm g I V partly esterified .with an aliphatic d ol selected from the 1111188 6561 avmgamoarraio of 1.0/0. 5/0.5 /0.5 01 respectively: g i conslstrmgv of ethyleng glycol n nevqperntyl FY Q chlorendic acid, phthallc acid, penan (2 a solvent for said ester. 7 I a 4 $5 gggg f g g iggfgg g 3. The curing agent solution of claim Zwherein' the solvents and treated withpercent polyol is selected from the group consisting of pentae gfi gg gg i gi f as rythritol, dipentaerythritol, and tripentaerythritol," the o 8.21325 olingolwlvdesisgigi a(5gr0axr;ft1y 1.25 140 non-chlorinated polycarboxylic. acid is selected from'the' minated ester having a molar ratio group consisting of phthahc ac1d, lsophthalic acid, tetragiicl.gflg/O.igfifiipggtgrelyi gilloreghydrophthalic acid and hexahydrophthalic acid and the mob andpsombmzed {,P 1,, f chlorinated polycarboxylic acid is selected from the group gg fgigs ff g gf gifg ggg fi g consisting of hexachloroendomethylenetetrahydrophthalic illustrated in Exam le I. acid-and tetrachlorophthalic acid. 4. A coating composition vehicle comprising EXAMPLE V I (a) an epoxidized fatty acid chain consisting of mate- I Additional tests performed in the manner of Example Tlals from i group Consisting of epoifidiltidv IV and illustrating the improved pot-life of epoxidized Challl fatty aclds andestefS thereof havmg oils catalyzed with the novel esters of this invention are 40 Iodine value of at least 90" before epoxidation-and.

tabulated below: 'after epoxidation containing not less than 4 percent Moles chlorendie acid 1. 0 1. 0 1. 0 0 1. 0 1. 0 l 0 l 0 Moles phthalic anhydride 0. 9 0. 9 0. 9 9 0. 9 Moles tetrahydrophthalic anhydride 0 9 0. 9 0. 9 Moles pentaery thritol 0. 0 5 O. 5 0. 5 Percent by weight ethylene glycol. 3. 3. 9 Percent by weight neopentyl glycol 3. 9 3. 9 3. 9 Acid v ue 9 96 99 95 98 98 99 Drying time tacktree, Hours.-. 5 5 1. 0 2. 2. 5 2 5 Gel time, Hours- 184 164 115 78 94 184 120. Time of glycol addition 1 I Time of glycol addition indicates whether the glycol was added initially with other reactants or was added finalllyhte after substantial esterification had been efiected. Y

Final.

From the tests of the above samples, it is noteworthy oxirane groups located within the molecules of said that the curing agents (carboxyl terminated esters) treated fatty acid chainmaterial, p V with a diol gave catalyzed epoxidized oils having con- (b) a curingagent having freecarboxyl groups comconsiderably better pot-life without any apparent decrease prising an ester prepared from an aliphatic polyol in cure time. having a hydroxyl-functionality from about 2' to All of the above films were cured at room temperature about 6 and containing 3 to about 15 carbon atoms, and all the films when fully cured were hard, mar-resista nonchlorinated mononuclear cyclic p'olycarboxylic ant, and solvent resistant. acid having 6 cyclicjcarbon atoms and a chlorinated While specific examples of the invention have been set cyclic polycarboxylic' acid having at'least 6 cyclic forth hereinabove, it is not intended to limit the invencarbon atoms, said nonchlorinated ipolycarboxylic tion solely thereto, but to include all of the variations and acid being present in a ratio of moles of acidto modifications falling within the scope of the appended. equivalents of polyol of about 0.05:1 to abopt 0.75: 1, claim said chlorinated polycarboxylic acid being present We claim: in such quantity as to have a ratio of total moles 1. A curing agent solution for epoxide resins comprisof acid to equivalents of polyol of about 0.6:1 to, ing (1)" an ester prepared from a polyol containing from I about 1.211, wherein any nonchlorinated polycarabout 2 to about 6 hydroxyl groups, a nonhalogenated box'ylic acid unreact'ed with'said polyol is at least polycarboxylic acid containing 2 to about 12 carbon .partly esterified with an aliphatic diol selected from atoms, and a halogenated polycarboxylic acid containing the group consisting of ethylene glycol and neopentyl 3 to about 12 carbon atoms, said nonhalogenated polyglycol, and I carboxylic acid being present in a ratio of moles of acid (c) amutual solvent for (a) and (b). i

5. A method of preparing a curing agent solution of an ester of polyol containing from about 2 to about 6 hydroxyl groups, a nonhalogenated polycarboxylic acid containing 2 to about 12 carbon atoms, and a halogenated polycarboxylic acid containing 3 to about 12 carbon atoms comprising esterifying an admixture of polyol, nonhalogenated polycarboxylic acid, and halogenated polycarboxylic acid at a temperature of about 100 C. to about 250 C. in the presence of about 1.0 percent by weight to about 8.0 percent by weight of the reactants, an aliphatic diol having 2 to carbon atoms and solubilizing in a solvent for the ester, said nonhalogenated polycarboxylic acid being present in a ratio of moles of acid to equivalents of polyol of about 0.05 :1 to about 0.75 1, said halogenated polycarboxylic acid being present in such quantity as to have a ratio of total moles of acid to equivalents of polyol of about 0.6:] to about 1.2:1.

6. A method of preparing a curing agent solution of an ester of a polyol, a nonhalogenated polycarboxylic acid containing 2 to about 12 carbon atoms, and a halogenated polycarboxylic acid containing 3 to about 12 carbon atoms comprising:

(a) esterifying an admixture of polyol containing from about 2 to about 6 hydroxyl groups, nonhalogenated polycarboxylic acid, and halogenated polycarboxylic acid at a temperature of about 100 C. to about 250 C., said nonhalogenated polycarboxylic acid being present in a ratio of moles of acid to equivalents of polyol of about 0.05:1 to about 0.75:1, said halogenated polycarboxylic acid being present in such quantity as to have a ratio of total moles of acid to equivalents of polyol of about 0.6:1 to about 1.2:1,

(b) adding about 1.0 percent by weight to about 8.0 percent by weight of the reactants of an aliphatic diol of 2 to 10 carbon atoms at a temperature of about 140 C. to about 180 C., and

(c) solubilizing the ester in a solvent for the ester.

7. The method of claim 6 wherein the esterification of polyol, nonhalogenated polycarboxylic acid and halogenated polycarboxylic acid is conducted at a temperature of about 140 C. to about 250 C.

8. The method of claim 6 wherein the polyol is selected from the group consisting of pentaerythritol, dipentae- 'rythritol, tripentaerythritol, the nonhalogenated polycarboxylic acid is selected from the group consisting of phthalic acid, isophthalic, tetrahydrophthalic acid, and hexahydrophthalic acid, and the halogenated polycarboxylic acid is selected from the group consisting of hexachloroendomethylenctetrahydrophthalic acid and tetrachlorophthalic acid.

9. The method of claim 8 wherein the diol is selected from the class consisting of ethylene glycol and neopentyl glycol.

10. The method of claim 6 wherein the esterification is conducted in the presence of a solvent.

11. A method of preparing a curing agent solution of an ester of a polyol, a nonhalogenated polycarboxylic acid containing 2 to about 12 carbon atoms, and a halogenated polycarboxylic acid containing 3 to about 12 carbon atoms comprising:

(a) heating an admixture of polyol containing from about 2 to about 6 hydroxyl groups and nonhalogenated polycarboxylic acid to a temperature of about C. to about 250 C., said nonhalogenated polycarboxylic acid being present in a ratio of moles of acid to equivalents of polyol of about 0.05 :1 to about 0.75 :1, said halogenated polycarboxylic acid being present in such quantity as to have a ratio of equivalents of polyol of about 0.6:1 to about 1.2:1, wherein any nonhalogenated polycarboxylic acid unreacted with said polyol is at least partly esterified with an aliphatic diol having 2 to 10 carbon atoms,

(b) maintaining the temperature at about 100 C. to

about 250 C. while adding said halogenated polycarboxylic acid, said halogenated polycarboxylic acid being added in such quantity as to have a ratio of total moles of acid to equivalents of polyol of about 0.6:1 to about 1.2: 1, and

(c) solubiiizing the ester in a solvent for the ester.

12. The method of claim 11 wherein the mixture of polyol and nonhalogenated polycarboxylic acid is heated to a temperature of about C. to about 200 C. and the temperature is maintained at about 140 C. to about 200 C. while the halogenated polycarboxylic acid is added.

13. The method of claim 11 wherein the polyol is pentaerythritol, the nonhalogenated polycarboxylic acid is phthalic acid, and the halogenated polycarboxylic acid is hexachloroendomethylenetetrahydrophthalic acid.

14. The method of claim 11 wherein the diol is selected from the class consisting of ethylene glycol and neopentyl glycol.

15. The method of claim 11 wherein the admixture is heated in the presence of a solvent.

16. The method of claim 6 wherein the nonhalogenated polycarboxylic acid and the polyol are admixed initially and heated to a temperature of about 100 C. to about 250 C. prior to the addition of the halogen-containing polycarboxylic acid.

References Cited UNITED STATES PATENTS 3,018,258 l/l962 Meier et al 2602 3,050,480 8/1962 Budde 106252 3,269,853 8/1966 English 106252 ALLAN LIEBERMAN, Primary Examiner.

U.S. DEPARTMENT OF COMMERCE PATENT OFFICE Washington, D.C. 20231 UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No. 3,408,215 October 29, 1968 Marco Wismer et a1.

It is certified that error appears in the above identified patent and that said Letters Patent are hereby corrected as shown below:

In the heading to the printed specification, line 4, "Pittsburgh Plate Glass Company," should read PPG Industries Inc. Column 8, line 17 "to polyol" should read of polyol Signed and sealed this 10th day of March 1970.

(SEAL) Attest:

WILLIAM E. SCHUYLER, JR.

Commissioner of Patents Edward M. Fletcher, Jr.

Attesting Officer 

